Job Description
Design and develop new devices or elements of new devices with the intent of commercialization in accordance with Quality System Requirements. Participate as a technical lead on multiple cross-functional development teams managing projects from concept through commercialization. Design, assemble, and evaluate prototype devices/assemblies to assess technical feasibility of various solutions. Support accurate and efficient translation of user and patient needs into verified/validated devices by creating and refining design requirements, specifications, and test methods while adhering to design controls best practices.
ResponsibilitiesDevelop robust test methods and design test fixtures to accurately evaluate selected materials and prototype designs against specifications and requirements.Communicate deliverable status cross-functionally to facilitate the product development process.Serve as technical lead for projects/products, identifying, developing, and implementing solutions to complex problems.Interface professionally with physicians and other medical personnel while maintaining confidentiality and intellectual property vigilance.Author protocols and reports, including engineering studies using basic statistical methods.Communicate with outside suppliers for component and equipment sourcing and refinement.Assist or own verification and validation activities through regulatory clearance and design transfer, including building finished devices for verification/validation purposes.Contribute to design/development of product line extensions and product improvements.Mentor peers and junior engineers to advance R&D department technical ability and core competencies.Essential SkillsMedical device work history with 5+ years of experience.Strong understanding of ISO certifications.Product development from concept to commercialization.Solidworks CAD design.Mechanical engineering, injection molding, extrusion process, fixture design, tooling design.New product introduction and test method development.Project management skills.Additional Skills & QualificationsBachelor’s Degree in Engineering or related technical field and 5 years of related work experience.Familiarity with various materials and processes such as extrusion processing, injection molding, machine shop operations, fixtures, and tooling.Knowledge of adhesive and thermal bonding and various other processes for catheter fabrication and design.Skills in generating new product designs/concepts, catheter materials, processes, and design plus test methods and metrology.Knowledge of project management, documentation, design control methodology, and medical device regulations.Understanding of clinical applications and associated product requirements with the ability to translate these requirements into detailed specifications.Experience taking products through the development process to launch.Pay and Benefits
The pay range for this position is $100000.00 - $125000.00/yr.
Health & Wellness:
- Employer-subsidized health insurance.
- Employer-paid dental insurance.
- Employer HSA contribution.
- Gym membership subsidy.
Financial Security:
- 401k plan with company match.
- Employee Short Term Disability, Long Term Disability, and AD&D Life Insurance.
Time Off & Flexibility:
- 9 paid holidays (including your birthday!).
-PTO and Personal days.
Workplace Type
This is a fully onsite position in Minneapolis,MN.
Application Deadline
This position is anticipated to close on Aug 22, 2025.
About Actalent
Actalent is a global leader in engineering and sciences services and talent solutions. We help visionary companies advance their engineering and science initiatives through access to specialized experts who drive scale, innovation and speed to market. With a network of almost 30,000 consultants and more than 4,500 clients across the U.S., Canada, Asia and Europe, Actalent serves many of the Fortune 500.
The company is an equal opportunity employer and will consider all applications without regard to race, sex, age, color, religion, national origin, veteran status, disability, sexual orientation, gender identity, genetic information or any characteristic protected by law.
If you would like to request a reasonable accommodation, such as the modification or adjustment of the job application process or interviewing due to a disability, please email actalentaccommodation@actalentservices.com for other accommodation options.